chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13621681	13621682	T	C	18	GENIC	homozygous	142217921
10	13624921	13624922	C	T	12	GENIC	homozygous	142217922
10	13626881	13626882	C	G	18	GENIC	homozygous	138725961
10	13627115	13627116	C	T	15	GENIC	homozygous	142217923
10	13628219	13628220	C	T	25	GENIC	homozygous	142217924
10	13630817	13630818	C	G	21	GENIC	homozygous	142217925
10	13631732	13631733	C	A	19	GENIC	homozygous	142217926
10	13634265	13634266	A	G	15	GENIC	homozygous	142217927
10	13634979	13634980	G	A	18	GENIC	homozygous	142217928
10	13635394	13635395	A	G	20	GENIC	homozygous	142217929
10	13638245	13638246	G	A	21	GENIC	homozygous	142217930
10	13640527	13640528	A	G	13	GENIC	possibly homozygous	142217931
10	13640998	13640999	G	A	15	GENIC	homozygous	142217932
10	13641326	13641327	T	G	16	GENIC	homozygous	142217933
10	13641724	13641725	G	T	22	GENIC	homozygous	142217934
10	13645182	13645183	G	A	22	GENIC	homozygous	142217935
10	13647874	13647875	C	T	16	GENIC	homozygous	142217936
10	13653301	13653302	G	C	24	GENIC	homozygous	142217937
10	13653473	13653473		CA	14	GENIC	homozygous	142196778